A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610673



Internal ID21558978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47416784..47416784hg38UCSC Ensembl
chr3:47458274..47458274hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138293
SamplesHG02818
Known GenesSCAP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610673
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer